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在无标记基因情况下基于荧光对逆转录病毒转导细胞的筛选:对转导的B型尼曼-皮克病细胞的直接筛选及旁观者校正证据

Fluorescence-based selection of retrovirally transduced cells in the absence of a marker gene: direct selection of transduced type B Niemann-Pick disease cells and evidence for bystander correction.

作者信息

Yeyati P L, Agmon V, Fillat C, Dinur T, Dagan A, Desnick R J, Gatt S, Schuchman E H

机构信息

Department of Human Genetics, Mount Sinai School of Medicine, New York, NY 10029, USA.

出版信息

Hum Gene Ther. 1995 Aug;6(8):975-83. doi: 10.1089/hum.1995.6.8-975.

Abstract

Types A and B Niemann-Pick disease (NPD) are lysosomal storage disorders resulting from the deficient activity of acid sphingomyelinase (ASM). Type A NPD is characterized by the absence of residual ASM activity, massive accumulation of sphingomyelin and cholesterol within lysosomes, and a rapid, neurodegenerative course that leads to death by 3 years of age. In contrast, type B NPD patients have low, but detectable, levels of residual ASM activity and little or no neurologic disease. Thus, individuals with type B NPD may survive into late adolescence or adulthood and are considered excellent candidates for somatic cell gene therapy. To facilitate the development of gene therapy for this disorder, a novel procedure was devised to isolate metabolically corrected type B NPD cells in the absence of marker gene expression. Type B NPD cells were transduced with retroviral vectors expressing ASM, labeled with lissamine rhodamine sphingomyelin (LR-SPM), and subjected to preparative fluorescence-activated cell sorting (FACS). Two non-overlapping cell populations were isolated, corresponding to enzymatically corrected (i.e., low fluorescence) and noncorrected (i.e., high fluorescence) cells. Quantitative PCR analysis demonstrated that the enzymatically corrected cells were enriched for vector sequences. Moreover, the corrected cells could be regrown and continued to express high levels of ASM activity after numerous passages, consistent with the fact that they were stably transduced. Notably, coculture of FACS-sorted, overexpressing cells with untreated type B NPD fibroblasts resulted in a homogeneous cell population with low fluorescence whose FACS distribution overlapped that of the corrected cells. Computerized fluorescence microscopy confirmed that nearly all of these cocultured cells expressed ASM activity and could hydrolyze LR-SPM.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

A型和B型尼曼-匹克病(NPD)是由酸性鞘磷脂酶(ASM)活性不足导致的溶酶体贮积症。A型NPD的特征是缺乏残余ASM活性,溶酶体内鞘磷脂和胆固醇大量蓄积,以及快速的神经退行性病程,通常在3岁前死亡。相比之下,B型NPD患者有低水平但可检测到的残余ASM活性,几乎没有神经疾病。因此,B型NPD患者可能存活至青春期后期或成年期,被认为是体细胞基因治疗的理想候选者。为了促进针对这种疾病的基因治疗的发展,设计了一种新方法,在不表达标记基因的情况下分离代谢校正的B型NPD细胞。用表达ASM的逆转录病毒载体转导B型NPD细胞,用丽丝胺罗丹明鞘磷脂(LR-SPM)标记,然后进行制备性荧光激活细胞分选(FACS)。分离出两个不重叠的细胞群体,分别对应酶校正(即低荧光)和未校正(即高荧光)的细胞。定量PCR分析表明,酶校正的细胞富含载体序列。此外,校正后的细胞可以再生长,并且在多次传代后继续表达高水平的ASM活性,这与它们被稳定转导的事实一致。值得注意的是,将FACS分选的过表达细胞与未处理的B型NPD成纤维细胞共培养,产生了一个低荧光的均匀细胞群体,其FACS分布与校正后的细胞重叠。计算机化荧光显微镜证实,几乎所有这些共培养的细胞都表达ASM活性,并且能够水解LR-SPM。(摘要截断于250字)

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